| |
| Device | OVATION ABDOMINAL STENT GRAFT SYSTEM |
| Classification Name | system, endovascular graft, aortic aneurysm treatment |
| Generic Name | system, endovascular graft, aortic aneurysm treatment |
| Applicant |
| TRIVASCULAR INC |
| 3910 brickway blvd |
| santa rosa, CA 95403 |
|
| PMA Number | P120006 |
| Date Received | 04/11/2012 |
| Decision Date | 10/05/2012 |
| Product Code | |
| Docket Number | 12M-1110 |
| Notice Date | 11/08/2012 |
| Advisory Committee |
Cardiovascular |
| Clinical Trials |
NCT01092117
|
| Expedited Review Granted? | No |
| Combination Product |
No
|
| Recalls |
CDRH Recalls
|
Approval Order Statement
APPROVAL FOR THE OVATION ABDOMINAL STENT GRAFT SYSTEM. THIS DEVICE IS INDICATED FOR TREATMENT OF PATIENTS WITH ABDOMINALAORTIC ANEURYSMS HAVING VASCULAR MORPHOLOGY SUITABLE FOR ENDOVASCULAR REPAIR, INCLUDING: 1) ADEQUATE ILIAC/FEMORAL ACCESS COMPATIBLE WITH VASCULAR ACCESS TECHNIQUES, DEVICES, AND/OR ACCESSORIES; 2) NON-ANEURYSMAL PROXIMAL AORTIC NECK: A) WITH A LENGTH OF AT LEAST 7 MM PROXIMAL TO THE ANEURYSM; B) WITH AN INNER WALL DIAMETER OF NO LESS THAN 16 MM AND NO GREATER THAN 30 MM; AND C) WITH AN AORTIC ANGLE OF <= 60 DEGREES IF PROXIMAL NECK IS >= 10 MM AND <=45 DEGREES IF PROXIMAL NECK IS <10 MM. 3) ADEQUATE DISTAL ILIAC LANDING ZONE: A) WITH A LENGTH OF AT LEAST 10 MM; AND WITH AN INNER WALL DIAMETER OF NO LESS THAN 8 MM AND NO GREATER THAN 20 MM. |
| Approval Order |
Approval Order
|
| Summary |
Summary of Safety and Effectiveness
|
| Labeling |
Labeling
|
| Post-Approval Study | Show Report Schedule and Study Progress |
| Supplements: |
S001 S003 S004 S005 S006 S007 S008 S009 S010 S011 S013 S014 S015 S016 S017 S018 S019 S020 S021 S023 S024 S025 S026 |